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The Leaflex™ Brazilian Standalone Study

Aortic Valve Stenosis Clinical Trial

Official title:
The Leaflex™ Brazilian Standalone Study

Clinical Trial Summary

A prospective, multicenter, single-arm study aimed to demonstrate safety and performance of the Leaflex™ Performer in the treatment of symptomatic severe aortic stenosis. Subjects will be seen at pre- and post procedure, discharge, 30 days and at 3, 6, 9 and 12 months post procedure.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05052684
Study type Interventional
Source Pi-cardia
Contact
Status Active, not recruiting
Phase N/A
Start date October 3, 2022
Completion date December 31, 2024
View Details
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